Abstract
In an effort to identify tumor-specific antigens recognized by CD4+ T cells, an approach was developed that allows the screening of an invariant chain-complementary DNA fusion library in a genetically engineered cell line expressing the essential components of the major histocompatibility complex (MHC) class II processing and presentation pathway. This led to the identification of a mutated form of human CDC27, which gave rise to an HLA- DR4-restricted melanoma antigen. A mutated form of triosephosphate isomerase, isolated by a biochemical method, was also identified as an HLA-DR1- restricted antigen. Thus, this approach may be generally applicable to the identification of antigens recognized by CD4+ T cells, which could aid the development of strategies for the treatment of patients with cancer, autoimmune diseases, or infectious diseases.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 1351-1354 |
| Number of pages | 4 |
| Journal | Science |
| Volume | 284 |
| Issue number | 5418 |
| DOIs | |
| State | Published - May 21 1999 |
ASJC Scopus subject areas
- General
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